The author is a student of B.Sc. (HONS) Physics, at GC University, Faisalabd, Pakistan. This Dissertation submitted in partial fulfillment of the Requirement of the Degree of B.Sc. (H) Physics. She completed her project under the venerable supervision of her supervisor Prof. M. Attiq Khan Shahid, Department of Physics, GC University Faisalabad.
Biological investigations report that there are several disease processes involving factors of environmental pollution. Pollution has direct effects on lungs, causes lung diseases and indirect effects on all parts of the body. Here, an attempt has been made to study the effects of pollution on hepatitis, the inflammation of liver. Nitric oxide is suggested to play a primary role in vasodilatation. The diagnostic methods of choice for diagnosing the disease are enzymes and antibody detection tests including ALT test, ALP test, Bilirubin test, PCR test, etc. It is a progressive disease with poor outcomes. No effective medical treatment exists and vaccination is the treatment of choice.
Keeping in view, the above said discrepancy attempt has been made in this study to co-relate the Environmental Pollution with Hepatitis, so that the control of Environmental Pollution may help in reducing the intensity of the above mentioned disease.
For that purpose, the data of hepatitis patients was collected in specially selected hospitals and analyzed for the determination of the environmental hepatitis. For the confirmation of these experimental findings, a sociological survey was conducted accordingly. 100 people were selected for that purpose. Questionnaires were distributed among them, and collected back after the prescribed limit of time. The data provided by them was analyzed statistically and co-relation was found positive.
A detailed study of hepatitis and the people living near the environmentally polluted areas with respect to air, water, land, marine and industrial pollution revealed that hepatitis viruses infected most of the people.
God has made this universe and we, as a creature for some purpose and set a balance and symmetry in every thing. All the things around us such as plants, water, air, animals, etc. makes our environment.
The relationship between human and his environment is a two way process. If one disturbs, other will be automatically the victim. Therefore, the present work has been taken to illustrate the impact of ill environmental health on the health of human beings in respect of hepatitis.
The environment provides man with the essential life support systems, which comprises air, water and land, but it also presents him a variety of hazards, which may prejudice his health.
The World Health Organization recognizes that Health is the fundamental right of every man without distinction of race, religion, political belief, economic and social conditions. While every effort is being made in attaining this conception, much remains to be done.
The WHO has defined “Health” as a “State of Physical, Mental and Social well-being and not merely the absence of disease and infirmity”. It represents a balanced relationship of the body and mind and complete adjustment to the total environment.
Health signifies a soundness of body and mind but we are confronted with the difficulty of determining its relationship to disease. Health and disease must be intimately related for if disease did not exist it would be irrelevant to talk of health.
Disease may be called as an abnormal state of body resulting from harmful effects of processes, injurious substances or accidents. In general, “disease is a state of body in which certain natural functions are so disturbed that the individual cannot meet the usual requirements of life”. On the other hand, “disease is maladjustment or maladaptation in an environment, a reaction for the worse between man and hazards or adverse influences in his external environment.” The response of the individual to these influences is conditioned by his genetic make-up or internal environment.
Environmental pollution may be described as the unfavorable alteration of our surroundings attributed to the anthropogenic activities of man. Environmental pollution takes place through changes in energy patterns, radiation levels, chemical and physical constitution and abundance of microorganisms. Pollution included release of materials into the atmosphere, which make the air unsuitable for breathing, harm the quality of water and soil, and give out substances which damage the health of human beings, plants and animals. Though the other environmental pollutants, odour and noise only disturb the cell function, they can also some times be a danger to health. The effects of pollution to our biosphere are numerous and are increasing alarmingly.
The pathway of impact of the environment in the human body evidently are the systems that are exposed to hazardous materials, covering the external skin and the internal respiratory and alimentary systems, each with an array of organs and functions, and with an ultimate bearing on the structures and organs of the body as a whole.
It was not until the middle of the 19th century that man’s understanding of nature grew that he could bring the major environmental health hazards to his control. Another half-century later achievements of sanitary engineering and preventive medicine in adapting the environment to man were complemented by the success of therapeutic medicine in helping man to conquer some of the diseases.
It is interesting to note that health has direct relation to environment. Several diseases have a direct relation to environmental management. The environmental components involved in communicable diseases such as malaria, schistosomiasis, filariasis and trypanosomiasis. Also many other ailments like asthma and allergy are known to be environment linked. The efforts to control these diseases through environmental interventions directed at the habitats of their vector have come in for considerable attention. But the large scale use particularly in developing countries, of growth promoting substances to increase concern about chronic toxic effects in human beings, which might ultimately be related to cancer with incidence affecting the skin, mouth, lungs, liver, kidney, breast, vascular systems, etc. Among these growth-promoting substances are antibiotics, hormones and vitamins.
The relationship between cancer in different parts of the body and various environmental contaminant and pollutants, have been increasingly observed over a long period. Keeping in view this effect of cancer, a study was conducted at Allied Hospital, Faisalabad, related to different kinds of cancer and was found correct.
(Ref: Mini Project titled “Effects of Environmental Pollution on cancer ”, written by “Teyaba Kanwal” under supervision of “Prof. M. Attiq Khan Shahid”)
Viruses | Types of Cancers |
Hepatitis B Virus (HBV) | Hepatocellular carcinoma |
Human Papillomaviruses (HPV) | Cervical and other anogenital carcinomas |
Squamous cell skin carcinomas | |
Epstein-Barr virus (EBV) | Burkitt’s and other B-cell lymphomas |
Nasopharyngeal carcinomas | |
Human T-cell lymphotropic Viruses (HTLV-1) | Adult T-cell leukemia |
Human immunodeficiency Virus (HIV) | Lymphomas, Kaposi’s sarcoma, anogenital carcinomas |
Hepatitis B virus causes Hepatocellular carcinoma, a type of cancer. So that it is observed that Hepatitis and cancer correlate to each other.
It is now generally agreed that between 60 and 90 percent of all cancers are directly or indirectly related to the environment, that is, related to factors, in water, air, solar radiation, living and working environments and personal choices of diet and ways of life such as tobacco smoking and alcohol consumption. The assumption is that all cancers are environmentally caused until it can be proved otherwise.
Viewing the world as a whole, the net effects of many known cancer-causing factors remain substantial, though none is as prominent as tobacco. The Table 2.2 given enlists causes of cancer.
Factors | Percentage of all cancer death | |
Best estimate | Range of acceptable estimate | |
Tobacco | 30 | 25 – 40 |
Alcohol | 03 | 02 – 04 |
Diet | 35 | 10 – 70 |
Food additives | < 1 | -5 – 2 |
Reproductive and sexual behavior | 7 | 01 – 13 |
Occupation | 4 | 02 – 08 |
Pollution | 2 | < 1 – 5 |
Industrial products | < 1 | < 1 – 2 |
Medicines and medical procedures | 1 | 0.5 – 3 |
Geophysical factors | 3 | 02 – 04 |
Infection | 10 – ? | 1 – ? |
Hepatitis is a general term used to describe inflammation of the liver. This means that there are too many inflammatory chemicals being produced and released in the liver, which damages the liver cells.
Hepatitis commonly results from a virus, particularly one of the five hepatitis viruses — A, B, C, D, or E (a sixth category called hepatitis virus G had been created but has since been retracted). Less commonly, hepatitis can be caused by excessive alcohol, toxic chemicals, incorrect diet, some drugs such as paracetamol, autoimmune diseases, poisons, non-viral infections like Q fever, and various viral infections including glandular fever as well as some diseases of the biliary system.
Hepatitis can be acute (short-lived) or chronic (lasting at least 6 months). It is common throughout the world.
Hepatitis A virus (HAV) is an RNA virus. The virus is present in blood and bowel movements for two to three weeks before any symptoms develop and for two to three weeks afterward. During this time, the hepatitis A virus can infect anyone who handles anything contaminated by blood or feces.
Hepatitis A is the commonest type of viral hepatitis and occurs worldwide. Hepatitis A is also known as infectious hepatitis. The virus attacks the liver producing an acute illness. This illness usually lasts for several weeks and resolves quickly once the virus is cleared from the body. Occasionally the illness recurs within three months after the initial episode. Those who have been infected develop antibodies that protect against further episodes of hepatitis A. In those who are run down to start with there may be a prolonged or relapsing illness and this occurs in around 15% of cases. However unlike hepatitis B or C, a chronic illness does not develop from the hepatitis A virus, and once the virus is cleared from the body a permanent immunity is acquired. Hepatitis A virus does not cause a carrier state or chronic hepatitis.
Most hepatitis A infections cause no symptoms and go unrecognized, though within two to five weeks, susceptible persons who have acquired the virus will develop any or all of the following symptoms:
The duration and severity of the symptoms vary with each individual and usually disappear gradually after four to six weeks.
Hepatitis A occurs more frequently in developing countries and lower socioeconomic groups, possibly because of overcrowding and poor sanitation. All people who live in the household with an individual who has hepatitis A should be:
Generally, people with hepatitis A recover well. However, it can sometimes be fatal and it may take a long while to feel really well again. Most cases of Hepatitis A are self-limited and resolve spontaneously. Hepatitis A does not progress to chronic liver disease.
Hepatitis B is a deadly liver disease caused by virus B. Hepatitis B virus (HBV) is a DNA virus, which is an important cause of acute and chronic liver disease worldwide with the highest incidence rates in Far East (15%) and the Mediterranean (5%). It can lead to long-term liver complications like cirrhosis, cancer and ultimately death. Globally, Hepatitis B causes about two million deaths every year and there are 350 million carriers of the virus. It is responsible for 80% cases of liver cancer. Viral Hepatitis kills more people than cancer or any other infectious disease.
It is 100 times more dangerous than AIDS. In Pakistan every 10th person is carrying Hepatitis B virus without any symptom and can transmit this disease to other persons.
Hepatitis B is highly contagious during the four to six weeks before symptoms appear and for a variable period afterwards. Type B hepatitis is often more severe than type A and has a longer incubation time. The incubation period is 2 – 4 months.
The Hepatitis B surface antigen appears early in the course of the disease and may persist for several months. If this surface antigen remains positive after 6 months from the onset of disease, it will likely persist indefinitely and the individual will become a chronic carrier of Hepatitis B. Up to 10% of patients with acute Hepatitis B will develop chronic hepatitis, which can result in cirrhosis (scarring of the liver) or liver cancer. It is the ninth major cause of death.
Hepatitis B virus can survive outside the body for long periods of time. There are approximately 300 million new infections of Hepatitis B per year in the world.
There are three major factors involved in the transmission of Hepatitis B. Hepatitis B is commonly transmitted sexually, through IV needles, or from mother to infant. Hepatitis B is less easily transmitted than Hepatitis A. Transmission commonly occurs through:
At increased risk of transmission are people in closed environments because body fluid contact is more likely such as:
It is noted that still there are many cases of Hepatitis B having no known source.
The symptoms of hepatitis B are the same as those of hepatitis A but tend to be more severe and longer lasting. After initial contact with the virus symptoms take on average, around 60 to 90 days to develop. Persons will develop symptoms that vary in severity from mild to full-blown, and include:
Joint pains and itchy red hives on the skin are more likely in a person with hepatitis B than with the other viruses.
Also it may be happened that there are no symptoms of the virus in a carrier person and carrier one may infect others without knowing it.
Prevention against Hepatitis B is crucial. Since 1983 a vaccine against hepatitis B has been available. This vaccine is made using techniques of genetic engineering. Vaccination is a good idea for those who are at a high risk of catching hepatitis B. High risk people are health care workers, haemodialysis patients, low socioeconomic groups, homosexual men, injection drug users, prostitutes, the sexually promiscuous, infants and children of immigrants from disease-endemic areas, infants born to infected mothers, sexual and household contacts of infected persons. Because hepatitis B is such a widespread infection it is recommended that children be routinely vaccinated against this virus.
Vaccination against hepatitis B stimulates the body’s immune defenses and protects most people. However, people undergoing dialysis, people with cirrhosis, and people with an impaired immune system may derive less protection from vaccination.
Recovery without any long-term effects is the usual outcome. Those who make a recovery have a good immune system, which eradicates the virus for life.
In a small percentage of people the virus remains in the body long-term and is infectious to others. These people are known as carriers. This chronic form of hepatitis B may silently damage your liver as the years go by, and a significant percentage of chronic carriers will develop liver cancer or cirrhosis.
With hepatitis B, about 1 percent will develop a rapidly progressive life-threatening Hepatitis; some go on to develop chronic hepatitis and about 5 percent become symptom-free carriers. Liver cancer can also be a complication of hepatitis B and C. It is frequent in those (fortunately few) hepatitis B sufferers who have developed established cirrhosis secondary to chronic active hepatitis.
Hepatitis C is caused by a collection of viruses that belong to neither the type A nor type B disease. Hepatitis C virus (HCV) is an RNA virus, which was responsible for 90% of post transfusion hepatitis until screening of donor blood was introduced. This virus, which is sometimes difficult to identify, causes most of the hepatitis spread through blood transfusions. Previously it was known as non-A, non-B hepatitis till it identified. Hepatitis C often has a more prolonged course than A and B.
Hepatitis C virus (HCV) is classed as the fastest-growing infectious disease in Australia and America, and this upward trend is set to continue through out the world. If it does, by the year 2010 we can expect many thousands of people to have developed HCV- related cirrhosis, with many requiring liver transplants. It is an epidemic problem. Infection with the hepatitis C virus is common, and there are around 300 million people worldwide who have contracted this virus.
Researchers estimate that in Australia, 1% to 3% of the general population tests positive to hepatitis C virus. In the USA the incidence is estimated to be around 2.8% of the population, while in many parts of Asia infection rates are much higher than this. HCV was only identified in 1988. It is 10 times more infectious than HIV, and unpublished research in Victoria suggests it may survive for long periods on needles and other equipment. In the 1980’s, AIDS was the major public health challenge for community-based doctors. Now Hepatitis C has this dubious honor.
People are generally completely unaware that they have contracted this virus because it does not produce any symptoms in the early or acute stages of the infection. During the first 3 to 6 months after infection, the virus replicates itself rapidly and the immune system tries to fight it by producing antibodies against it. Unfortunately in 80 to 85 percent of infected people, the virus is not eliminated and becomes a long-term inhabitant of the body. In other words, the infection becomes chronic. In a significant percentage of people with chronic infection, there are no signs or symptoms of disease and many are unaware that they are carrying an infection that can be transmitted to others through contact with their blood.
Hepatitis C is transmitted mainly by:
Also it is noted that:
Previous researches illustrated that HCV is not transmitted by:
Cocaine snorting is recognized increasingly as a potential mode of transmission through the sharing of contaminated straws.
In about 10 to 15 percent of cases no definite risk factor is detected and the mode of transmission remains unclear.
Hepatitis C is somewhat unpredictable. The acute illness is usually mild and often without symptoms. The symptoms are similar to those of hepatitis A and hepatitis B, but are often milder and may not include jaundice.
Initially the patient feels unwell with symptoms such as:
After one to two weeks the patient frequently becomes jaundiced (the skin and eyes turn yellow), and the symptoms then often improve. Most hepatitis C sufferers, however, do not develop this jaundice.
The urine may become dark and the bowel motions pale.
Many infected persons with HCV have no symptoms. In about 10 to 15 percent of cases no definite risk factor is detected and the mode of transmission remains unclear.
No vaccine is currently available. Standard immune globulin is not useful. However, precautions reduce the chances of catching the disease. The hepatitis C (and also Hepatitis B) patients must take the following precautions:
The amount of long term liver damage caused by the hepatitis C virus varies from person to person, and those with a strong immune system and a healthy diet and lifestyle will have a much better outcome.
Hepatitis D occurs in the context of Hepatitis B and still is uncommon in the world.
Hepatitis delta virus (HDV) is a defective RNA virus, which depends on hepatitis delta virus replication. It occurs as a co-infection with Hepatitis B virus or as a super infection causing an acute exacerbation of chronic Hepatitis B virus infection. Cirrhosis develops in 50 -70% of those who develop chronic HDV.
Hepatitis D occurs most often among people who share needles to inject illicit drugs.
Symptoms are mostly same as that of Hepatitis B but when a person with Hepatitis B has Hepatitis D as well, symptoms are more severe.
Vaccination against hepatitis B virus eliminates the risk of hepatitis D virus as well. Hepatitis B immune globulin also protects against hepatitis D infection.
Hepatitis E, enterically transmitted virus, yet has not been found common in the world.
Hepatitis E is spread primarily from the stool of one person to the mouth of another. It causes occasional epidemics, which are often waterborne, similar to those caused by hepatitis A virus. So far, these epidemics have occurred only in underdeveloped countries.
Hepatitis E may produce severe symptoms of acute viral hepatitis, especially in pregnant women. Chronic hepatitis or a chronic carrier state does not occur.
No vaccine is currently available. The usefulness of standard immune globulin is not known.
Ongoing research should lead to a clearer understanding of the natural history and epidemiology of Hepatitis D and Hepatitis E.
Pollution may be defined as the introduction by man in to the environment of substances or energy liable to cause hazards to human health, harm to living resources and ecological systems, damage to structure or amenity, or interference with legitimate use of the environment.
Pollutants have various alternative systems for their classification. Mainly pollutants are classified on the basis of their:
In this research report, we discuss the pollution classification by environmental sector only, because this research is only linked to environmental pollution.
Environmentally, we can classify the pollutants in the following categories.
The major air pollution is caused by fuel combustion in primary gases states like: Carbon dioxide, carbon monoxide, un-burned hydrocarbons, oxides of nitrogen, sulphur dioxide and Aldehydes. While there reaction caused forming secondary derivatives in form of Peroxy acetyl nitrates, oxides of nitrogen form ozone and sulphur dioxide brings acid rains, and particulate in gases form like: smoke, grit and dust, lead particles.
The air pollutants come from the following sectors:
Air pollution is confined mostly to cities and industrial areas. Solid and liquid waste areas resulted due to human and industrial activities. The quality of in-land surface and ground water reserves are deteriorating very fast due to indiscriminate release of un-treated municipal and industrial effluents and productivity of solid and is decrease due to over cropping, mono-cropping and indiscriminate use of farm chemicals.
These chemicals and toxic waste in a liquid form may not obstruct the drain but cause hazards like emissions of toxic gases, erosion of drain lining, which pose danger to public health. Dumping of solid and insoluble wastes in the drain results in the obstruction to the drainage and sewer lines which also result in to water-logging an spilling of waste water, which increases water borne diseases like hepatitis, amoeboisis, gastro-enteritis and typhoid.
The pollutants, which enter the water en-route, are:
The following are the pollutants usually found in water.
The major types of marine pollution are as under:
Water pollution is mainly caused by sewerage and industrial discharge, and wastewater drain in to rivers or channels.
Land pollution can be divided into the following sectors:
Due to land pollution food borne pollution reported arsenic (As) about 2-10ppm, which is enough to kill aquatic life. The maximum allowable levels of arsenic in food and water are 3.5 mg/kg and 0.05 ppm.
From industries we get pollution in gases form like organic vapors, chloro-fluro compounds, acids aerosols, aldehyde, fluoride, chloride and bromides. While we get heavy emission of particulars comes from industries are explain as under:
Radiation pollution is the radiation emitted or leaked by nuclear power plant. These radiation cause skin cancer, leukemia, induce mutation and change genetic order and cause related diseases.
Noise pollution mostly caused by the road, rail, air-traffic, industries, construction, public work, indoors noise pollution are caused due to ventilation system, office machines, catering trade, live or recorded music and domestic animals. Most of the acoustical energy of speech is in the frequency range of 100 Hz-6KHz, most important cue-bearing energy being between 300 Hz-3KHz. Noise above 80 dB (A), may reduce helping behavior and increase aggressive behavior. The heavy noise pollution results as chaemic heart disease, hypertension, mental illness, neurosis, increase level of stress hormones, sleep disturbance etc.
These are as under:
In Environmental Pollution we are concerned wit the poisons that occur in the ambient environment to which human beings may be exposed. This involves exposures to the pollutants in the workplace and food chain as well as natural and man-made activities.
There are three major routs to exposure of hazardous materials which includes:
This is the rout of entry of contaminants in the body, which deals with eating. Foods or other swallowed material are carried directly into the digestive system and they are metabolized.
Pollutants are carried away through out the body to the target areas where effects are felt.
Ingestion of hazardous material and its effect depends upon the solubility of the pollutants as they occur in food. Fat- soluble or lipophilic chemicals like DDT and Benzene are quickly absorbed in body through ingestion. Water-soluble chemicals or hydrophilic can also be absorbed in human body due to the reason that human metabolism is water based chemistry.
Chemical reactions of gastric fluid with pollutants can alter the solubility of the hazardous materials, their transpiration and metabolism in body.
Inhalation is the major rout of entry of the poison materials/pollutants in the body. It involves absorption of air born chemicals during the breathing. Absorption of certain chemicals in blood depends upon its solubility. These pollutants via lungs enter in the blood and can go directly to brain, liver, and rest of the body, e.g. CO, NO, vapors of Hg, etc.
Carbon monoxide has several hundred times binding affinity for hemoglobin. Nitric oxide has primary role in vasodilatation of lungs.
Retention of airborne pollutants depends upon particle size due to structure of lungs. The smaller sized pollutants penetrate deeper and have a great effect.
This is the entry of the pollutants in the body via absorption through skin. Those areas of the skin are in contact with chemical contaminants/pollutants are mostly effected.
Dermal absorption is enhanced by scratched, broken, roughened or abraded surfaces of the skin on ankles, hands, and neck or facial areas.
The response of the body to pollutants is to attempt to:
These are done by metabolism and the principal site for this detoxification is the liver.
In case when dose of certain pollutants becomes too large to be detoxified, these act as systematic poisons and target various organs. Some examples of systematic poisons and their target areas are indicated in table 2.3.
Systematic Poisons | Target Organs | Examples |
Heaptotoxic agents | Liver | · Carbon tetrachloride · Tetrachloroethane |
Nephrotoxic agents | Kidneys | · Halogenated · Hydrocarbons |
Haematopoietic toxic agents | Blood | · Aniline · Toluene · Nitrobenzene · Benzene · Phenols |
Neurotoxic agents | Nerve system | · Methanol · Carbon disulphide · Metals · Organomettalics |
Anaesthetics/Narcotics | Consciousness | · Acetylene hydrocarbons · Olefin · Ethyl ether, Isopropyl ether · Paraffin hydrocarbons · Aliphatic ketones · Aliphatic alcohols · Esters |
Liver is very serious target organ for cancer being center of metabolic activities, which changes the nature of the pollutants. e.g. Carbon tetrachloride due to metabolic activities of liver is absorbed and damaged it spontaneously.
Since lungs are in constant contact with Environment, they are most quickly affected of all the body organs to pollutants. As we go deeper in lungs structure, it becomes narrower and presents more tortuous paths, which offer an aerodynamic obstruction to particle movements.
Skin serves to keep pollutants, chemicals and microorganisms outside the body. The skin accomplishes this action by presenting to the “outside world” an oil based layer, which does not allow the water-based environmental pollutants to penetrate. But advanced and modern technology has introduced oil or solvent based chemicals. These fat-soluble chemicals are absorbed in lipophilic layers of skin, e.g. gasoline.
The eyes can be affected by the splashes of acids and alkalis, solid particles, ultraviolet and ionizing radiation.
Brain, spiral column and nerves can be damaged by dissolved heavy metals, e.g. Mercury and Lead.
Main function of the kidneys is to concentrate the pollutants and is affected by heavy metals and halogenated hydrocarbons.
Aromatic compounds like benzene and toluene and phenolic compounds can poison the blood.
Any pollutant when brings a change in DNA activity, it will change cell division, transmission of genes and ultimately reproductive system. e.g. Lead and diethylstilbestrol (DES).
Recently it was shown that there is a correlation between exhaled NO and alkaline phosphates, AST, ALT, Albumin and Billirubin (enzymes or protein synthesized by liver involves in the prediction of liver diseases e.g. Hepatitis) suggesting induction of NO synthesis by agents normally metabolized in liver.
NO has a primary role in vasodilatation and it is a vasodilator with regulatory action of vascular tone in humans.
In one study it was observed that exhaled NO is increased in decompensated liver cirrhosis, while those with compensated liver cirrhosis, chronic active hepatitis and normal control patients had the same amount of exhaled NO.
It seems that increased NO production is due to induction of NO synthesis within pulmonary endothelial cells by some stimulatory factors secreted by diseased liver or hypertensive portal system.
Cardiac index also correlated with NO level, revealing the role of NO in systemic circulatory disturbance.
More than 80% of patients present with signs and symptoms of liver disease but in about18%, the presenting symptoms and signs are relates to lung disease.
Selenium oxide is another vasodilator and has direct effect on liver and hence caused a liver disease. Selenium basically is a mineral that prevents the liver from diseases but when it reacts with oxygen and forms selenium oxide, it changes it chemical properties and become toxicant for the body organs especially liver.
There are a wide variety of body responses to environmental pollutants that are of concern in the field of poisonous material management.
Carcinogens are those pollutants, which may cause cancer. On the average, cancers are considered approximately 15% related to genetic effects and 85% related to environmental effects.
Mutagens are agents that cause genetic damage in reproductive cells. They are acted by alternation of DNA structure of the genes and effects are felt by the next generation. Radiation exposure is probably the most powerful example of a mutagenic effect.
Teratogens are the agents that adversely effect off springs while in the fatal stage of development. Thus offspring would be most likely to experience a teratogenic effect due to exposure of mother to an environmental pollutant. A well-documented case of such a teratogenic effect was the birth effects found in children of women who ingested thalidomide-containing pills in the early 1960s. It had developed effect on offspring during fatal period. Other teratogenic substances include alcohol, CO, anesthetic gases and diethylstilbestrol (DES).
Synergism can be the best summarized by saying two plus two equals five. This describes the enhancing effect of two different environmental pollutants up to the human body. For instance, asbestos may cause cancer, but the carcinogenic effect of asbestos is 240 times greater with a person who also smokes. Similarly narcotic effect of alcohol is greatly enhanced in the presence of carbon tetrachloride.
Saying two can best summarize antagonism plus two equals three. In an antagonistic effect, one impact is lessened in the presence of other substance. One may find that eating bread before drinking alcohol modifies the immediate effect of alcohol as compared to not eating bread with or prior to alcohol ingestion.
Another important concept to pollutant effect is the latency period. This is the time between first exposure on an individual to an environmental pollutant and clinical manifestation of an adverse effect. For human it varies from 20 to 40 years. Asbestosis (cancer of lungs) is the prime example of latency. Workers involved in shipbuilding during World War 2, were exposed to airborne asbestos fibers at very high concentration but it took 20-30 years after exposure to show up the effect (cancer). Hepatitis is also an example of latency. Arsenic, a hazardous pollutant involves in the hepatitis (cancer of liver).
As this report contains two different types of studies. So we have two different types of diagnostic methods. One is for Hepatitis and other for Environmental Pollution.
This section describes a wide variety of options of tests that are available to diagnose the Hepatitis. It does not advocate application of the entire range in all population. In some settings, only some of the options may be relevant and enough to diagnose the disease. In all settings, the goal is to arrest the disease by any means to provide the need of treatment.
Mostly there are used blood tests or LFT’s (including ALT, ALP, billirubin and PCR tests), which are responsible for the prediction of hepatitis. However some other tests are also used to diagnose the disease e.g. antibody tests, CT – scan, liver ultrasound, liver biopsy etc.
Liver Function Tests (LFTs) are used for the ongoing monitoring of hepatitis positive people. There are two aspects to liver function testing. The first is signs of liver injury. When liver cells are damaged or killed the enzymes that exist inside the cell to do work leak out into the blood stream. We can measure this. Because cells are dying and being replaced constantly, there is a little of the enzyme in your blood all the time. The amount present goes up when viral infection, toxic chemicals or alcohol, etc are injuring the liver. These enzymes have a ‘normal range’. It is only when the amount present exceeds the normal range that it clearly indicates ongoing liver damage. To complicate the issue, some people with normal liver enzymes (LFTs) also have ongoing damage. Signs of liver failure can also be observed through blood tests results.
How it is done?
No special preparation is required before having a blood test. Talk to your health professional about any concerns you have regarding the need for the test, its risks, or how it will be done.
The health professional drawing blood, will wrap an elastic band around your upper arm to temporarily stop the flow of blood through the veins of your arm. This makes it easier to put the needle into a vein properly because the veins below the band get larger and do not collapse easily.
The needle site is cleaned with alcohol, and the needle is inserted. More than one needle stick may be needed if the needle does not get placed correctly or if the vein cannot supply enough blood.
When the needle is properly placed in the vein, a collection tube will be attached to the needle and blood will flow into it. Sometimes more than one tube of blood is collected.
When enough blood has been collected, the band around your arm will be removed. A gauze pad or cotton ball is placed over the puncture site as the needle is withdrawn. Pressure is applied to the puncture site for several minutes and then a small bandage is often placed over it.
It is a type of blood test. It is the first laboratory sign of Hepatitis B and C infection.
Basically ALT is an enzyme or a type of protein that is synthesized by liver. By blood test we see its quantity present in liver either that is normal or not. Normally ALT presents in human blood in the range of 9 – 40 mg/dl. But if its quantity in blood differs that would be the sign of the presence of the disease. In most cases its quantity leaks from a damaged liver.
It is another type of blood test. ALP is another enzyme that indicates the presence of the disease.
ALP is an enzyme or protein synthesized by the liver in large amount when there is obstruction of the bile ducts to the normal flow of bile.
By blood test we measure its amount in laboratory to assess the function of liver. Normally in human blood ALP present in the range of 80 – 300 mg/dl and in case of hepatitis it increases in blood.
Basically billirubin is a chemical breakdown product of hemoglobin (the red blood cells). It is also measured by blood test.
We take some specimen of blood and measure the amount of billirubin in that specimen of blood in the laboratory to assess the liver function and find the presence of the disease.
Normally a human blood contains 1 mg/dl of billirubin, 0.25 mg/dl is present as a direct source and 0.75 mg/dl as an indirect source. In the presence of the disease the amount of billirubin decreases in blood.
PCR is a genetic base test used to amplify the genetic material of the virus to a level that can be detected the disease. PCR tests look for actual virus in the blood. It is useful when antibody and enzyme tests are unclear. This is a DNA like test by which we can predict the presence of hepatitis. It is the viral load that the PCR tests for. It is often required to have these tests done to confirm a diagnosis.
In simple words it is virus detection based test and used to analyze the virus.
PCR testing is technologically difficult and very easily contaminated, so tests should be done on a fresh blood specimen, which has not already been tested. The test amplifies up the tiny amounts of virus, which are present in the blood of an infected person. In the early days, there were major problems with quality of PCR tests and variability between laboratories. It is much more reliable nowadays but as always, no test is 100% fail safe and results need to be looked at in context and with a critical eye. There are three types of PCR.
It is another type of blood test used to diagnose the disease. GGT is the liver enzyme that has been traditionally used as a marker of excess alcohol intake. If your GGT is up at all, you should consider giving up alcohol altogether whilst you are infected with hepatitis specially hepatitis B and C. People with elevated GGT tend not to respond well to interferon. If GGT is over 100 or so, it can also be associated with gastro-intestinal symptoms (nausea, bloating, appetite disturbance and wind). Some people also have itching of the skin, the result of impairment to bile flow associated with bile duct damage, which is reflected in the elevated GGT. Your doctor can measure your bile acid levels and type on a regular blood specimen. These symptoms may be alleviated by the use of a medication called urso-deoxycholic acid (USDA), which is a ‘friendly’ bile acid and protects your bile ducts from ongoing damage. This medication is available on application to the ‘special access drug scheme’.
Blood serum contains large amounts of protein. Two major groups of proteins in blood serum are albumin and globulin.
A total serum protein test measures the total amount of protein in blood serum as well as the amounts of albumin and globulin. The amounts of albumin and globulin can help a doctor diagnose certain diseases e.g. hepatitis. In blood serum total range of serum protein is 5.5 – 9 g/dl.
AST is another type of blood test to measure the amount of AST in the blood to diagnose the disease.
AST is an enzyme or protein synthesized by liver and decrease in its synthesis predicts the presence of the disease.
It is an initial screening test for Hepatitis tests for the antibodies to the virus so it does not look directly for the virus itself.
An antibody is a protein produced by your body as a defense against the virus. We make antibodies against any organism that gets into our body and we also produce antibodies when we are vaccinated for measles, flu, hepatitis B, polio etc.
Positive antibody test suggests the presence of some form of autoimmune illness.
Sometimes this test comes back intermediate and then a repeat test is required. Antibodies are produced in the body after exposure to the virus and have produced antibodies to fight it.
It does not determine whether or not someone still has the virus or how long he or she has been infected. It takes up to 6 months for antibodies to hepatitis virus to form in the blood. This up take is called as seroconversion. It is therefore important to get retested 6 months after initial antibody test.
A CT (or CAT) scan is the term used to describe a radiologic test known as "computerized tomography" (or computed axial tomography). The CT scanner is a doughnut-shaped machine that uses advanced x-ray technology to take pictures of cross-sections of your body.
CT scan provides anatomic information about liver such as size and shape of the liver.
CT scanners use x-rays. For your safety, the amount of radiation is kept to an absolute minimum and our equipment is kept in top shape.
How it is done?
The CT scanner looks like a large donut with a narrow table in the middle, in which you would be placed inside the tunnel of the scanner. When undergoing a CT, you rarely experience claustrophobia because of the openness of the doughnut shape of the scanner. For CT scan of liver, you lie on your back on the table, which moves through the center of the machine.
You must remain motionless for the length of the study, which is typically just a few minutes. The entire procedure, which includes set-up, the scan itself, checking the pictures, and removing the IV needle if needed, takes 15-45 minutes.
As part of your test, before or during the study, you may be given an injection (by a nurse, technologist or doctor) of a contrast agent. This allows the radiologist to obtain clearer images of the organ.
Ultrasound scanning or sonography is a method of obtaining images from inside the human body through the use of high-frequency sound waves. The reflected sound wave echoes are recorded and displayed as a real-time visual image. No ionizing radiation (x-ray) is involved in ultrasound imaging.
Ultrasound is a useful way of examining many of the body’s internal organs, including but not limited to the heart, liver, gallbladder, spleen, pancreas, kidneys and bladder. Because ultrasound images are captured in real time, they can show movement of internal tissues and organs and enable physicians to see blood flow and heart valve functions. This can help to diagnose a variety of organ conditions during and after illness.
Just like CT scan it also provides anatomic information about the liver, such as size and shape of the liver. The only difference between the two techniques is the use of ionizing radiation (x-ray). In CT scan x-rays are used but in ultrasound scanning this technique in not involved.
How it is done?
Ultrasound scanners consist of a console containing a computer and electronics, a video display screen and a transducer that is used to scan the body. The transducer is a small hand-held device about the size of a bar of soap, attached to the scanner by a cord. The physician or technologist spreads a lubricating gel on the patient’s abdomen in the area being examined and then presses the transducer firmly against the skin to obtain images.
The ultrasound image is immediately visible on a nearby screen that looks much like a computer or television monitor. The physician or technologist watches this screen during an examination and captures representative images for storage. Often, the patient is able to see it as well.
In liver ultrasound, the patient is asked to be positioned on an examination table. A clear gel is applied to the patient’s body in the area to be examined to help the transducer make secure contact with the skin. The sound waves produced by the transducer cannot penetrate air so the gel helps eliminate air pockets between the transducer and the skin. The technologist or radiologist presses the transducer firmly against the skin and sweeps it back and forth to image the area of interest.
A liver biopsy is a procedure whereby small pieces of liver tissue are removed in order to be examined signs of damage or disease of the liver. It is very helpful in the diagnosis of diseases that affect the liver.
The physician decides to do a liver biopsy after tests suggest that the liver does not work properly. For example, a blood test might show that your blood contains higher than normal levels of liver enzymes or too much iron or copper. An x-ray could suggest that the liver is swollen. Looking at liver tissue itself is the best way to determine whether the liver is healthy or what is causing it to be damaged.
How it is done?
Liver biopsy is considered minor surgery, so it is done at the hospital. For the biopsy, you will lie on a hospital bed on your back with your right hand above your head. After marking the outline of your liver and injecting a local anesthetic to numb the area, the physician will make a small incision in your right side near your rib cage, then insert the biopsy needle and retrieve a sample of liver tissue. In some cases, the physician may use an ultrasound image of the liver to help guide the needle to a specific spot.
You will need to hold very still so that the physician does not nick the lung or gallbladder, which are close to the liver. The physician will ask you to hold your breath for 5 to 10 seconds while he or she puts the needle in your liver. You may feel pressure and a dull pain. The entire procedure takes about 20 minutes.
In liver biopsy a physician may take help of the CT scan or Ultrasound scanning to locate right the needle in the liver as there might be the chances of the misplace of the needle.
This section describes the method to determine the concentration of collected particulate matter randomly selected sites from mixed Faisalabad environment covering industrial, commercial and residential areas in order to have the air quality standards to diagnose the Environmental Pollution.
Kimoto High Volume air sampler was used for the collection of suspended particulate matter in the atmosphere of randomly selected areas of Faisalabad city. The high volume air sample used to pump large volume of air up to 2000 m³ at a rate of 0.8 m³.min-1. The filter used in a high volume air sample was glass fiber filter. Which have a collection efficiency of 99% for particles.
Samples were collected for a period of 12 Hrs (720 min) at an average flow rate of 0.8 m³.min-1. Particulate matter was trapped on each filter. Triplicate samples were collected from each place.
Kimoto High Volume air sampler was used for the sampling purpose. A high flow rate (0.8 m³.min-1) draw the air sample through a covered housing 20*25 cm rectangular glass fiber filters. The covered housing is necessary to protect the filter from precipitation & falling debris. Glass fiber filter was used because of their gradual head loss build up characteristics and non-hygroscopic properties. Contamination or damage to filter was avoided while inserting or removing then from the sampler. On removing from the each sampler it was folded in such a way that surface containing the deposits faced each other. The filter was weighed before and after sampling. (Anil, 1994).
The weight of each sample from each selected area was calculated by weighing the filter before sampling and after sampling.
The net weight of particulates was obtain by the formula:
W = W2 – W1
W = net weight of particulate matter for each sample
W1 = weight of filter before sampling
W2 = weight of filter after sampling
the net weight of particulate matter for each sample (which is obtained by subtracting W1 to W2).
Standard 1: 60 – 150
Standard 2: 75 – 260
Sr. # | Amount of Pollutants (μg/m³) | Areas |
1 | 350 | Residential cum Industrial |
2 | 425 | Residential cum Industrial |
3 | 275 | Residential cum Commercial |
4 | 680 | Residential cum Commercial |
5 | 267 | Residential cum Commercial |
6 | 283 | Residential cum Commercial |
7 | 390 | Residential |
8 | 250 | Safe Zone |
Sr. # | Month | No. of effected patients | |
Hep B | Hep C | ||
1. | October 2004 | 2 | 6 |
2. | November 2004 | 3 | 12 |
3. | December 2004 | 1 | 14 |
4. | January 2005 | 1 | 8 |
5. | February 2005 | 1 | 17 |
6. | March 2005 | 4 | 17 |
Total | Months 6 | 12 | 74 |
x | x‾ | (x - x‾) | (x – x‾)² |
12 | 2 | 10 | 100 |
74 | 12.34 | 61.66 | 3801.96 |
Standard Deviation = S.D = N / √n = (74 – 12) / √6 = 25.32
Mean Standard Deviation = σm = σ / √n = 25.32 / 2.45 = 10.34
Co-efficient of Variance = C.V = (σ / x‾) * 100 = (25.32 / 7.17) * 100 = 353.14
Probable Error = 0.67√n = 0.67 * 2.45 = 1.64
Relative Probable Error = .067 / √n = 0.67 / 2.45 = 0.274
Sr. # | Month | No. of effected patients | |
Hep B | Hep C | ||
1. | October 2004 | 1 | 11 |
2. | November 2004 | 6 | 12 |
3. | December 2004 | 1 | 18 |
4. | January 2005 | 3 | 12 |
5. | February 2005 | 5 | 14 |
6. | March 2005 | 6 | 16 |
Total | Months 6 | 22 | 83 |
x | x‾ | (x - x‾) | (x – x‾)² |
22 | 3.67 | 18.33 | 335.99 |
83 | 13.84 | 69.16 | 4783.11 |
Standard Deviation = S.D = σ = N / √n = (83 – 22) / √6 = 24.90
Mean Standard Deviation = σm = σ / √n = 24.90 / 2.45 = 10.17
Co-efficient of Variance = C.V = (σ / x‾) * 100 = (24.90 / 8.76) * 100 = 284.25
Probable Error = 0.67√n = 0.67 * 2.45 = 1.64
Relative Probable Error = .067 / √n = 0.67 / 2.45 = 0.274
Sr. # | Area | Total Respondent | No. of effected patients | |
Hep B | Hep C | |||
1. | Industrial | 49 | 19 | 48 |
2. | Industrial cum Commercial | 17 | 8 | 17 |
3. | Commercial | 9 | 3 | 8 |
4. | Commercial cum Residential | 7 | 2 | 6 |
Total | Areas 4 | 82 | 32 | 79 |
x | x‾ | (x - x‾) | (x – x‾)² |
32 | 8 | 24 | 576 |
79 | 19.75 | 59.25 | 3510.56 |
Standard Deviation = S.D = σ = N / √n = (79 – 32) / √4 = 23.50
Mean Standard Deviation = σm = σ / √n = 23.50 / 2 = 11.75
Co-efficient of Variance = C.V = (σ / x‾) * 100 = (23.50 / 13.88) * 100 = 169.31
Probable Error = 0.67√n = 0.67 * 2 = 1.34
Relative Probable Error = .067 / √n = 0.67 / 2 = 0.335
Year | Carcinomas Related to Lungs | Carcinomas Related to Other Body Organs |
2004 | 30 | 67 |
x | x‾ | (x - x‾) | (x – x‾)² |
30 | 15 | 15 | 225 |
67 | 33.5 | 33.5 | 1122.25 |
Standard Deviation = S.D = σ = N / √n = (67 – 30) / √2 = 26.16
Mean Standard Deviation = σm = σ / √n = 26.16 / √2 = 18.50
Co-efficient of Variance = C.V = (σ / x‾) * 100 = (26.16 / 24.25) * 100 = 107.87
Probable Error = 0.67√n = 0.67 * √2 = 0.94
Relative Probable Error = .067 / √n = 0.67 / √2 = 0.473
Sr. # | Std. Deviation σ | Mean Std. Deviation σm | Co-efficient of Invariance C.V | Probable Error P.E | Relative Probable Error R.P.E |
Hospital 1 | 25.32 | 10.34 | 353.14 | 1.64 | 0.274 |
Hospital 2 | 24.90 | 10.17 | 284.25 | 1.64 | 0.274 |
Mean | 25.11 | 10.25 | 318.69 | 1.64 | 0.274 |
Sr. # | Std. Deviation σ | Mean Std. Deviation σm | Co-efficient of Invariance C.V | Probable Error P.E | Relative Probable Error R.P.E |
Polluted Area | 23.50 | 11.75 | 169.31 | 1.340 | 0.335 |
Sr. # | Std. Deviation σ | Mean Std. Deviation σm | Co-efficient of Invariance C.V | Probable Error P.E | Relative Probable Error R.P.E |
Allied Hospital | 26.16 | 18.50 | 107.87 | 0.94 | 0.473 |
From our experimental findings, it is concluded that the concentration of ~90% samples was above International Standards, which confirms that Faisalabad Environment is highly polluted, and it may have adverse effects on human health.
Sites were selected using Syntax map method and SRS technique. A comprehensive questionnaire was designed for the sociological survey to obtain valid data. All copies of the questionnaire were distributed among the respondents by hand and collect personally. The respondents were asked to tick on “Yes” or “No” according to their choice of facts. The collected data was analyzed and presented in the tabular form.
Confirmation of diseases is completed through specific tests done at specially selected hospitals in Faisalabad. Those are:
Positive co-relationship between sociological data and experimental findings confirm our plan of study that Faisalabad environment is highly polluted and has adverse effects on human health, so it is strongly recommended that in these stations, the pollution quality management program may be initiated as early as possible meet the future demands. It is hoped that this data may helpful in developing future strategies and for comparison purposes with the other similar locations of the Industrial cum Commercial areas.
From this study it is also obvious that without the original causes of Hepatitis there are certain other factors involved in generating these diseases, which is the clear indication that environmental pollution may be the main cause of this disease.
The plan of the study under investigation was ”Environmental Pollution on Human Health in respect of Hepatitis-A case study”. The major objectives of the research report were to trace the causes of Hepatitis related to environmental pollution and find co-relationship between Hepatitis with Environmental pollution.
To achieve our goals, data of Hepatitis patients was collected is specially selected hospitals and analyzed for the determination of the environmental pollution.
To confirm these experimental findings, a survey was conducted at mixed environmental areas of Faisalabd, which are selected using Syntax map method and SRS technique. A comprehensive Questionnaire was designed with the help of supervisor for sociological survey to obtain valid data. 100 people were selected for the survey purpose from these areas. The Questionnaire was distributed among the respondents and collected back personally after a prescribed limit of time. The collected data was tabulated, analyzed and interpreted.
Most of the respondents confirmed that there are some factors of environmental pollution involved could cause Hepatitis in human beings. A small number of respondents denied experiencing any cause of Hepatitis but they were positive to the disease.
Positive co-relationship was found between sociological and experimental findings confirm our plan of study that “environmental pollution has adverse effects on human health in respect of Hepatitis”.
It was strongly recommended that in polluted areas the pollution quality management program might be initiated as early as possible to meet the future demands.
It was also recommended that control on Environmental Pollution might help in reduction of the intensity of the Hepatitis.
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